Welcome to our website. Here you will find a parents eye view of our day to day battle with Doose Syndrome (Myoclonic Astatic Epilepsy). It is all about my beautiful daughter Chloe, she is the bravest most inspiring person I know and I am totally in awe of how she manages to deal with her condition and to keep upbeat with a smile on her face.
Any views on this site are purely our own from our own experiences. Professional medical advice should be sought before commencing or changing any treatment.